EP3972959A1 - Neue catecholamin-prodrugs zur verwendung in der behandlung von morbus parkinson - Google Patents
Neue catecholamin-prodrugs zur verwendung in der behandlung von morbus parkinsonInfo
- Publication number
- EP3972959A1 EP3972959A1 EP20728430.8A EP20728430A EP3972959A1 EP 3972959 A1 EP3972959 A1 EP 3972959A1 EP 20728430 A EP20728430 A EP 20728430A EP 3972959 A1 EP3972959 A1 EP 3972959A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- compound
- propyl
- octahydrobenzo
- pharmaceutically acceptable
- disease
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
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- 125000001424 substituent group Chemical group 0.000 claims description 28
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
- C07D221/06—Ring systems of three rings
- C07D221/08—Aza-anthracenes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/5765—Six-membered rings condensed with carbocyclic rings or carbocyclic ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Definitions
- the present invention provides compounds that are phosphate, phosphonoxymethyl derivatives and ether derivative prodrugs of the dopamine agonist (4aR,10aR)-1-Propyl- 1,2,3,4,4a,5,10,10a-octahydro-benzo[g]quinoline-6,7-diol, and their use in the treatment of Parkinson’s disease and/or other conditions for which treatment with a dopamine agonist is therapeutically beneficial such as but not limited to Restless leg syndrome, Huntington’s disease and Alzheimer’s disease; and also neuropsychiatric diseases and disorders such as but not limited to schizophrenia, attention deficit hyperactivity disorder and drug addiction.
- Parkinson’s disease is a common neurodegenerative disorder that becomes increasingly prevalent with age and affects an estimated seven to ten million people worldwide. Parkinson’s disease is a multi-faceted disease characterized by both motor and non-motor symptoms. Motor symptoms include resting tremor (shaking), bradykinesia/akinesia (slowness and poverty of movements), muscular rigidity, postural instability and gait dysfunction; whereas non-motor symptoms include neuropsychiatric disorders (e.g.
- Parkinson’s disease pathophysiology is the loss of pigmented dopaminergic neurons in the substantia nigra pars compacta that provides dopaminergic innervation to the striatum and other brain areas. Such progressive neurodegeneration leads to the decrease in dopamine striatal levels which ultimately results in a series of changes in the basal ganglia circuitry, ultimately ending up in the occurrence of the four cardinal motor features of Parkinson’s disease.
- the main target of dopamine in the striatum consists of medium spiny GABAergic neurons (MSNs) selectively expressing D1 or D2 receptors pending topographical projections.
- GABAergic-MSN projecting to the external pallidum also called striato-pallidal ‘indirect pathway’ express D2 receptors (MSN-2); whereas GABAergic-MSN projecting to the substantia nigra pars reticulata and internal pallidum, also called striato-nigral‘direct pathway’ express D1 receptors (MSN-1).
- L-DOPA L-3,4-dihydroxy phenylalanine
- Other approaches consist in the administration of dopamine receptor agonists such as apomorphine which acts both on the D1 and D2 receptors subtypes, or pramipexole, ropinirole and others which are predominantly directed towards D2 receptors subtypes.
- Optimal motor relief is obtained with use of both L-DOPA and apomorphine due to their activation of both D1 and D2 receptor subtypes and holistic re-equilibrium of the indirect-direct pathways (i.e. while D2 agonists only reverse the indirect pathway dysfunction).
- L-DOPA and apomorphine with the structures depicted below are currently the most efficacious PD drugs in clinical use.
- L-DOPA is a prodrug of dopamine and remains the most efficacious drug in the treatment of motor Parkinson’s disease.
- complications arise due the inherent progression of the disease (i.e. sustained loss of dopaminergic neurons) as well as poor pharmacokinetic (PK) profile of L- DOPA.
- PK pharmacokinetic
- Those complications include: 1) dyskinesia which are abnormal involuntary movements occurring during the optimal‘on-time effect’ of the drug; and 2) off fluctuations, period during which the L-DOPA positive effect wears off and symptoms re-emerge or worsen (Sprenger and Poewe, CNS Drugs (2013), 27: 259-272).
- Direct dopamine receptor agonists are able to activate the dopamine auto receptors as well as the postsynaptic dopamine receptors located on the medium spiny neurons MSN-1 and MSN-2.
- Apomorphine belongs to a class of dopamine agonists with a 1,2-dihydroxybenzene (catechol) moiety. When combined with a phenethylamine motif, catecholamines often possess low or no oral bioavailability as is the case for apomorphine. Apomorphine is used clinically in PD therapy albeit with a non-oral delivery (typically intermittent subcutaneous administration or daytime continuous parenteral infusion via a pump). For apomorphine, animal studies have shown that transdermal delivery or implants may provide possible forms of administration.
- adrogolide undergoes extensive hepatic first-pass metabolism in man after oral dosing and, as a result, has a low oral bioavailability (app.4%).
- IV adrogolide has antiparkinson efficacy comparable to that of L-DOPA (Giardina and Williams; CNS Drug Reviews (2001), Vol.7 (3): 305-316).
- an alternative prodrug approach involves the masking of the two catechol hydroxyl groups as the corresponding methylene- dioxy derivative or di-acetalyl derivative.
- This prodrug principle has been described for example in Campbell et al., Neuropharmacology (1982); 21(10): 953-961 and in US4543256, WO 2009/026934 and WO 2009/026935.
- Yet another suggested approach for a catecholamine prodrug is the formation of an enone derivative as suggested in for example WO 2001/078713 and in Liu et al., Bioorganic Med. Chem. (2008), 16: 3438-3444.
- Compound (I) is a dopamine receptor agonist with mixed D1 and D2 activity.
- Three prodrug derivatives of compound (I) are known in the art. Liu et al., J. Med. Chem. (2006), 49: 1494-1498 and Liu et al., Bioorganic Med. Chem. (2008), 16: 3438-3444 disclose the enone derivative of formula (Ia) depicted below which was shown to be converted to the active compound (I) in rats.
- WO 2009/026934 and WO 2009/026935 disclose two types of prodrug derivatives of compound (I) including (6aR,10aR)-7-propyl-6,6a,7,8,9,10,10a,11-octahydro- [1,3]dioxolo[4',5':5,6]benzo[1,2-g]quinoline, a methylenedioxy (MDO) derivative with the formula (Ib) below:
- a prodrug derivative of a mixed D1/D2 agonist giving a stable PK profile which can provide continuous dopaminergic stimulation may fulfil such unmet needs.
- Phosphate derivatives as prodrug principle have previously been suggested and explored for various compounds including catechol moieties.
- EP0167204 discloses that oral absorption of L-DOPA could be improved by phosphorylation of one hydroxy phenol group. This was demonstrated by showing increased renal blood-flow in anesthetized dogs.
- US 3132171 discloses that diphosphate derivatization of L-DOPA provides a water soluble and stable composition which is converted to L-DOPA upon parenteral administration in rats.
- US 5073547 discloses monophosphorylated L-DOPA esters and suggests that these provides high bioavailability by the oral route (based on intraperitoneal dosing) which is suggested to be caused by decreased peripheral decarboxylation of the compounds. Lately, phosphate and bis-phosphate derivatives of carbidopa and levodopa with the aim of improving the aqueous solubility of these compounds has been disclosed in WO 2016/065019.
- Plasma concentration profiles of levodopa and carbidopa demonstrate conversion of phosphate derivatives of carbidopa and levodopa after intravenous and subcutaneous administration.
- Phosphonooxymethyl derivatization of amines has been suggested as a prodrug principle for amine compounds distinct from catecholamines.
- Masking of catechol hydroxy groups of carbidopa derivatives with benzyl or small alkyl for improvement of intestinal absorption has been suggested in WO 2004/052841 but prodrug potential of such compounds was not demonstrated.
- SUMMARY OF THE INVENTION The present invention relates to new compounds for treatment of Parkinson’s Disease.
- the invention relates to new prodrug derivatives of the compound (4aR,10aR)-1-n-Propyl-1,2,3,4,4a,5,10,10a-octahydro-benzo[g]quinoline-6,7-diol (compound (I)).
- the compounds of the invention have proven particularly useful for oral delivery of compound (I).
- the invention provides a compound according to formula (Id)
- R1, R2 and R3 are according to a) or b) below: a) R1 and R2 are each independently selected from H, C 1 -C 6 alkyl, benzyl and substituent (i) below, and R3 is absent,
- R4 and R5 are each independently selected from H, C 1 -C 6 alkyl, phenyl, benzyl, C 3 -C 6 cycloalkyl and methyl substituted with C 3 -C 6 cycloalkyl; or a pharmaceutically acceptable salt thereof.
- a pharmaceutical composition comprising a compound according formula (Id) or a pharmaceutically acceptable salt thereof, and one or more pharmaceutically acceptable excipients.
- Another aspect of the invention relates to a compound according to formula (Id) or a pharmaceutically acceptable salt thereof for use in the treatment of a neurodegenerative disease or disorder such as Parkinson's Disease, Huntington’s disease, Restless leg syndrome or Alzheimer’s disease; or a neuropsychiatric disease or disorder such as schizophrenia, attention deficit hyperactivity disorder or drug addiction.
- a neurodegenerative disease or disorder such as Parkinson's Disease, Huntington’s disease, Restless leg syndrome or Alzheimer’s disease
- a neuropsychiatric disease or disorder such as schizophrenia, attention deficit hyperactivity disorder or drug addiction.
- Another aspect of the invention relates to a method for the treatment of a neurodegenerative disease or disorder such as Parkinson's Disease, Huntington’s disease, Restless leg syndrome or Alzheimer’s disease; or a neuropsychiatric disease or disorder such as schizophrenia, attention deficit hyperactivity disorder or drug addiction; which method comprises the administration of a therapeutically effective amount of a compound of formula (Id) or a pharmaceutically acceptable salt thereof, to a patient in need thereof.
- a neurodegenerative disease or disorder such as Parkinson's Disease, Huntington’s disease, Restless leg syndrome or Alzheimer’s disease
- a neuropsychiatric disease or disorder such as schizophrenia, attention deficit hyperactivity disorder or drug addiction
- Another aspect of the invention relates to the use of a compound according to formula (Id) or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for the treatment of a neurodegenerative disease or disorder such as Parkinson's Disease, Huntington’s disease, Restless leg syndrome or Alzheimer’s disease; or for the treatment of a neuropsychiatric disease or disorder such as schizophrenia, attention deficit hyperactivity disorder or drug addiction.
- a neurodegenerative disease or disorder such as Parkinson's Disease, Huntington’s disease, Restless leg syndrome or Alzheimer’s disease
- a neuropsychiatric disease or disorder such as schizophrenia, attention deficit hyperactivity disorder or drug addiction.
- references to compounds encompassed by the invention includes the free substance (e.g. a free base or a zwitter ion) of compounds of the invention, pharmaceutically acceptable salts of compounds of the invention, such as acid addition salts or base addition salts, and polymorphic and amorphic forms of compounds of the invention and of pharmaceutically acceptable salts thereof.
- the compounds of the invention and pharmaceutically acceptable salts thereof may potentially exist in unsolvated as well as in solvated forms with pharmaceutically acceptable solvents such as water, ethanol and the like. Both solvated and unsolvated forms are encompassed by the present invention.
- Pharmaceutically acceptable salts Pharmaceutically acceptable salts in the present context is intended to indicate non- toxic, i.e. physiologically acceptable salts.
- pharmaceutically acceptable salts include pharmaceutically acceptable acid addition salts which are salts formed with inorganic and/or organic acids on the nitrogen atom in the parent molecule.
- Said acids may be selected from for example hydrochloric acid, hydrobromic acid, phosphoric acid, nitrous acid, sulphuric acid, benzoic acid, citric acid, gluconic acid, lactic acid, maleic acid, succinic acid, tartaric acid, acetic acid, propionic acid, oxalic acid, malonic acid, fumaric acid, glutamic acid, pyroglutamic acid, salicylic acid, gentisic acid, saccharin, and sulfonic acids such as methanesulfonic acid, ethanesulfonic acid, toluenesulfonic acid, naphthalene-2-sulphonic acid, 2-hydroxy ethanesulphonic acid and benzenesulfonic acid.
- pharmaceutically acceptable salts also include pharmaceutically acceptable base addition salts which are salts formed with inorganic and/or organic bases on the acidic groups of compounds of formula (Id).
- Said bases may be selected from for example zink hydroxide, and alkali metal bases, such as sodium hydroxide, lithium hydroxide, potassium hydroxide, and alkaline earth bases, such as calcium hydroxide and magnesium hydroxide, and organic bases, such as choline, diethylamine, trimethylamine and triethylamine. Additional examples of useful acids and bases to form pharmaceutically acceptable salts can be found e.g. in Stahl and Wermuth (Eds)“Handbook of Pharmaceutical salts. Properties, selection, and use”, Wiley-VCH, 2008.
- Prodrug indicates a compound that, after administration to a living subject, such as a mammal, preferably a human; is converted within the body into a pharmacologically active moiety.
- the conversion preferably takes place within a mammal, such as in a mouse, rat, dog, minipig, rabbit, monkey and/or human.
- a“prodrug of the compound (4aR,10aR)-1-n-Propyl- 1,2,3,4,4a,5,10,10a-octahydro-benzo[g]quinoline-6,7-diol” or“a prodrug of the compound of formula (I)” or“a prodrug of compound (I)” is understood to be a compound that, after administration, is converted within the body into the compound (4aR,10aR)-1-n-Propyl- 1,2,3,4,4a,5,10,10a-octahydro-benzo[g]quinoline-6,7-diol.
- Said administration may be by any conventional route of administration of pharmaceutical compositions known in the art, preferably by oral administration.
- the terms“parent compound” and“parent molecule” indicate the pharmacologically active moiety obtained upon conversion of a corresponding prodrug.
- the“parent compound” of one of the compounds (Ia), (Ib), (Ic) or any of the compounds of the invention is understood to be the compound of formula (I).
- Substituents in the present context a given range may interchangeably be indicated with“-“ (dash) or“to”, e.g. the term”C 1 -C 6 alkyl” is equivalent to”C 1 to C 6 alkyl”.
- the term”alkyl refer to a linear (i.e. unbranched) or branched saturated hydrocarbon having from one up to six carbon atoms, inclusive.
- cycloalkyl refers to a saturated ring system containing all carbon atoms as ring members and zero double bonds.
- a cycloalkyl may be a monocyclic cycloalkyl (e.g., cyclopropyl).
- Representative examples of cycloalkyl include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl.
- PK profile is an abbreviation of "pharmacokinetic profile”.
- Pharmacokinetic profiles and pharmacokinetic parameters described herein are based on the plasma concentration-time data obtained for the compound of formula (I) after oral dosing of a compound of the invention, using non-compartmental modelling.
- Abbreviated PK parameters are: C max (maximum concentration); t max (time to C max ); t 1 ⁇ 2 (half-life); AUC 0-24 (area under the curve from time of dosing and until 24 hours after dosing), and“Exposure at 24 h” is the plasma concentration of the compound of formula (I) as measured 24 hours after dosing.
- therapeutically effective amount of a compound of the invention means an amount sufficient to alleviate, arrest, partly arrest, remove or delay the clinical manifestations of a given disease and its complications in a therapeutic intervention comprising the administration of said compound.
- An amount adequate to accomplish this is defined as “therapeutically effective amount”.
- Effective amounts for each purpose will depend e.g. on the severity of the disease or injury as well as the weight and general state of the subject. It will be understood that determining an appropriate dosage may be achieved using routine experimentation, by constructing a matrix of values and testing different points in the matrix, which is all within the ordinary skills of a trained physician.
- a "therapeutically effective amount" of a compound of the invention indicates an amount of said compound of the invention that is able to provide an amount of compound (I) that is sufficient to alleviate, arrest, partly arrest, remove or delay the clinical manifestations of a given disease and its complications when said compound of the invention is administered, preferably by the oral route, to a mammal, preferably a human.
- Treatment and treating is intended to indicate the management and care of a patient for the purpose of alleviating, arresting, partly arresting, removing or delaying progress of the clinical manifestation of the disease.
- the patient to be treated is preferably a mammal, in particular a human being.
- the compounds of the present invention are intended for treatment of neurodegenerative diseases and disorders such as Parkinson’s disease and/or other conditions for which treatment with a dopamine agonist is therapeutically beneficial.
- Therapeutic indications include a variety of central nervous system disorders characterized by motor and/or non-motor disturbances and for which part of the underlying pathophysiology is a dysfunction of the striatal-mediated circuitry. Such functional disturbances can be seen in neurodegenerative diseases such as but not limited to Parkinson’s disease (PD), Restless leg syndrome, Huntington’s disease, and Alzheimer’s disease but also neuropsychiatric diseases such as, but not limited to schizophrenia, attention deficit hyperactivity disorder and drug addiction.
- the compounds of formula (Id) are for use as stand-alone treatment as the sole active compound.
- the compounds of formula (Id) may be used in combination with other agents useful in the treatment of a neurodegenerative disease or disorder such as Parkinson’s disease.
- a neurodegenerative disease or disorder such as Parkinson’s disease.
- the terms “combined use”,“in combination with” and“a combination of” and the like as used herein in the context of the method of the invention comprising the combined administration of therapeutically effective amounts of a compound of formula (Id), and another compound, which compound is useful in the treatment a neurodegenerative disease or disorder, is intended to mean the administration of a compound of formula (Id) simultaneously or sequentially, in any order, together with said other compound.
- the two compounds may be administered simultaneously or with a time gap between the administrations of the two compounds.
- the two compounds may be administered either as part of the same pharmaceutical formulation or composition, or in separate pharmaceutical formulations or compositions.
- the two compounds may be administered on the same day or on different days. They may be administered by the same route, such for example by oral administration, subcutaneous injection, by transdermal administration, by depot, by intramuscular injection or intravenous injection; or by different routes wherein one compound is for example administered orally or placed by depot and the other compound is for example injected.
- the two compounds may be administered by the same dosage regime or interval, such as once or twice daily, weekly, or monthly; or by different dosage regimes for example wherein one is administered once daily and the other is administered twice daily or weekly or monthly.
- the patient to be treated may already be in treatment with one or more other compounds useful in the treatment of a neurodegenerative disease or disorder when treatment with a compound of formula (Id) is initiated.
- the patient may already be in treatment with a compound of formula (Id) when treatment with one or more other compounds useful in the treatment of a neurodegenerative disease or disorder is initiated.
- the treatment with a compound of formula (Id) and treatment with one or more other compounds useful in the treatment of a neurodegenerative disease or disorder is initiated at the same time.
- compounds to be used in combination with a compound of formula (Id) may be selected from for example L-DOPA, droxidopa, foliglurax, MAO-B inhibitors such as selegiline or rasagiline, COMT inhibitors such as entacapone or tolcapone, adenosine 2a antagonists such as istradefylline, antiglutamatergic agents such as amantadine or memantine, acetylcholinesterase inhibitors such as rivastigmine, donepezil or galantamine and antipsychotic agents such as quetiapine, clozapine, risperidone, pimavanserin, olanzapine, haloperidol, aripiprazole or brexpiprazole.
- MAO-B inhibitors such as selegiline or rasagiline
- COMT inhibitors such as entacapone or tolcapone
- adenosine 2a antagonists such as is
- compositions comprising a compound of formula (Id), either as the sole active compound or in combination with another active compound, may be specifically formulated for administration by any suitable route such as the oral, rectal, nasal, buccal, sublingual, pulmonal, transdermal and parenteral (e.g. subcutaneous, intramuscular, and intravenous) route.
- the oral route is the preferred route of administration. It will be appreciated that the route will depend on the general condition and age of the subject to be treated, the nature of the condition to be treated and the active ingredient.
- excipient or“pharmaceutically acceptable excipient” refers to pharmaceutical excipients including, but not limited to, carriers, fillers, diluents, antiadherents, binders, coatings, colours, disintegrants, flavours, glidants, lubricants, preservatives, sorbents, sweeteners, solvents, vehicles and adjuvants.
- the present invention also provides a pharmaceutical composition comprising a compound of formula (Id), such as one of the compounds disclosed in the Experimental Section herein.
- the present invention also provides a process for making a pharmaceutical composition comprising a compound of formula (Id).
- compositions according to the invention may be formulated with pharmaceutically acceptable excipients in accordance with conventional techniques such as those disclosed in Remington,“The Science and Practice of Pharmacy”, 22 th edition (2013), Edited by Allen, Loyd V., Jr.
- the pharmaceutical composition comprising a compound of the present invention is preferably a pharmaceutical composition for oral administration.
- Pharmaceutical compositions for oral administration include solid oral dosage forms such as tablets, capsules, powders and granules; and liquid oral dosage forms such as solutions, emulsions, suspensions and syrups as well as powders and granules to be dissolved or suspended in an appropriate liquid.
- Solid oral dosage forms may be presented as discrete units (e.g.
- the solid dosage forms may be prepared with coatings such as enteric coatings or they may be formulated so as to provide modified release of the active ingredient such as delayed or extended release according to methods well known in the art.
- the solid dosage form may be a dosage form disintegrating in the saliva, such as for example an orodispersible tablet.
- excipients suitable for solid oral formulation include, but are not limited to, microcrystalline cellulose, corn starch, lactose, mannitol, povidone, croscarmellose sodium, sucrose, cyclodextrin, talcum, gelatin, pectin, magnesium stearate, stearic acid and lower alkyl ethers of cellulose.
- the solid formulation may include excipients for delayed or extended release formulations known in the art, such as glyceryl monostearate or hypromellose.
- the formulation may for example be prepared by mixing the active ingredient with solid excipients and subsequently compressing the mixture in a conventional tableting machine; or the formulation may for example be placed in a hard capsule e.g. in powder, pellet or mini tablet form.
- the amount of solid excipient will vary widely but will typically range from about 25 mg to about 1 g per dosage unit.
- Liquid oral dosage forms may be presented as for example elixirs, syrups, oral drops or a liquid filled capsule. Liquid oral dosage forms may also be presented as powders for a solution or suspension in an aqueous or non-aqueous liquid.
- excipients suitable for liquid oral formulation include, but are not limited to, ethanol, propylene glycol, glycerol, polyethylenglycols, poloxamers, sorbitol, poly-sorbate, mono and di-glycerides, cyclodextrins, coconut oil, palm oil, and water.
- Liquid oral dosage forms may for example be prepared by dissolving or suspending the active ingredient in an aqueous or non-aqueous liquid, or by incorporating the active ingredient into an oil-in-water or water-in-oil liquid emulsion. Further excipients may be used in solid and liquid oral formulations, such as colourings, flavourings and preservatives etc.
- compositions for parenteral administration include sterile aqueous and nonaqueous solutions, dispersions, suspensions or emulsions for injection or infusion, concentrates for injection or infusion as well as sterile powders to be reconstituted in sterile solutions or dispersions for injection or infusion prior to use.
- excipients suitable for parenteral formulation include, but are not limited to water, coconut oil, palm oil and solutions of cyclodextrins.
- Aqueous formulations should be suitably buffered if necessary and rendered isotonic with sufficient saline or glucose.
- Other types of pharmaceutical compositions include suppositories, inhalants, creams, gels, dermal patches, implants and formulations for buccal or sublingual administration.
- the excipients used for any pharmaceutical formulation comply with the intended route of administration and are compatible with the active ingredients.
- the compound of the present invention is administered in an amount from about 0.0001 mg/kg body weight to about 5 mg/kg body weight per day.
- daily dosages may be in the range of 0.001 mg/kg body weight to about 2 mg/kg body weight per day. The exact dosages will depend upon the frequency and mode of administration, the sex, the age, the weight, and the general condition of the subject to be treated, the nature and the severity of the condition to be treated, any concomitant diseases to be treated, the desired effect of the treatment and other factors known to those skilled in the art.
- a typical oral dosage for adults will be in the range of 0.01-100 mg/day of a compound of the present invention, such as 0.05-50 mg/day, such as 0.1-10 mg/day or 0.1-5 mg/day.
- the compounds of the invention are administered in a unit dosage form containing said compounds in an amount of about 0.01 to 50 mg, such as 0.05 mg, 0.1 mg, 0.2 mg, 0.5 mg, 1 mg, 5 mg, 10 mg, 15 mg, 20 mg or up to 50 mg of a compound of the present invention.
- FIGURES Figure 1 graphic illustration of conversion of compounds to the invention to compound (Id). Solid arrows: conversion demonstrated in vitro and in vivo. Dotted arrow: conversion demonstrated in vitro.
- Figure 2 PK profiles in Wistar rats obtained after oral dosing according to Example 3. Profiles are based on mean plasma concentrations from 3 subjects for each compound.
- X-axis time (hours);
- Y-axis plasma concentration of Compound (I) (pg/mL) obtained after dosing of the following compounds: ⁇ : compound (Ia); ⁇ : compound (Ib); +: compound (9); ⁇ : compound (8); X: compound (3) and ⁇ : compound (2).
- the inventors have identified new compounds that are prodrugs of (4aR,10aR)-1- Propyl-1,2,3,4,4a,5,10,10a-octahydro-benzo[g]quinoline-6,7-diol [compound (I)] which is a dual D1/D2 agonist (see for example WO 2009/026934).
- the compounds of the invention are phosphate and phosphonoxymethyl derivatives and ether derivatives of compound (I). It was found that oral dosing of representative compounds of the invention in Wistar rats provides a systemic exposure of compound (I) in plasma, suggesting the usefulness of said compounds as orally active prodrugs of compound (I).
- the doses were corrected by molecular weight to equal a dose of 300 ⁇ g/kg of compound (Ib) corresponding to 287 ⁇ g/kg of compound (I). It has been observed that oral dosing of compounds (Ia) and (Ib) to Wistar rats results in early and high peak plasma concentrations of compound (I). Such high peak concentrations are in humans likely to be associated with dopaminergic side effects such as for example nausea, vomiting and light headedness. In contrast, for the compounds of the invention a slower absorption rate was observed accompanied by a sustained exposure of compound (I) avoiding rapid peak concentrations.
- the plasma exposure of compound (I) in Wistar rats is maintained throughout 24 hours although the obtained AUC of compound (I) is generally lower than the AUC obtained after dosing of compounds (Ia) and (Ib).
- the peak concentrations of compound (I) which are expected to drive the side effects are lower, higher doses might be administered of the compounds of the invention to potentially achieve higher overall plasma concentrations of compound (I) compared to what is achievable from dosing compounds (Ia) and (Ib).
- PK properties of compound (Ic) the inventors found that the plasma concentrations of compound (I) were extremely low, leaving compound (Ic) unsuitable as a prodrug of compound (I) for oral administration and confirming that the oral bioavailability of the compounds of the invention is highly unpredictable.
- PK parameters for the PK studies in Wistar rats are listed in Table 4 and PK profiles are depicted in Figure 2. All the compounds evaluated in vivo showed conversion to compound (I). The phosphate and phosphoonoxymethyl derivatives are preferred embodiments of the invention. Bioconversion of the compounds of the invention to the compound of formula (Id) has also been assessed by incubation in human plasma and/or human hepatocytes as described in Example 1. For the parent compound (I) itself a short half-life in the plasma assay was observed, which likely explains why appearance of compound (I) was in some instances difficult to detect or only detected in very small amounts as compound (I) may have been metabolised at the same time as it was formed.
- the compounds of the invention are useful as orally active prodrugs of compound (I) and has been observed in rats to provide a PK profile avoiding the peak Cmax observed for the known prodrugs (Ia) and (Ib) and providing a significantly higher AUC of compound (I) than compound (Ic).
- an important issue associated with the compound (Ib) is that this compound is an agonist of the 5-HT2B receptor.
- 5-HT2B receptor agonists have been linked to pathogenesis of valvular heart disease (VHD) after long term exposure, such compounds are not suitable for use in the treatment of chronical diseases (Rothman et al., Circulation (2000), 102: 2836-2841; and Cavero and Guillon, J. Pharmacol. Toxicol. Methods (2014), 69: 150-161).
- a further advantage of the compounds of the invention is that these are not 5-HT2B agonists c.f. example 2 and Table 3.
- the compounds of the invention are useful in the treatment of neurodegenerative diseases and disorders such as Parkinson’s disease and/or other conditions for which treatment with a dopamine agonist is therapeutically beneficial.
- the compounds being suitable for oral administration have the potential of providing a new treatment paradigm in Parkinson’s Disease.
- the compounds are for use as stand-alone treatment of a neurodegenerative disease or disorder.
- the compounds are to be used in combination with other agents for treatment of PD such as a compound selected from the group consisting of L-DOPA, droxidopa, foliglurax, a MAO-B inhibitor such as selegiline or rasagiline, a COMT inhibitor such as entacapone or tolcapone, an adenosine 2a antagonist such as istradefylline, an antiglutamatergic agent such as amantadine or memantine, an acetylcholinesterase inhibitor such as rivastigmine, donepezil or galantamine, an antipsychotic agent such as quetiapine, clozapine, risperidone, pimavanserin, olanzapine, haloperidol,
- R1, R2 and R3 are according to a) or b) below: a) R1 and R2 are each independently selected from H, C1-C6 alkyl, benzyl and substituent (i) below, and R3 is absent,
- R4 and R5 are each independently selected from H, C 1 -C 6 alkyl, phenyl, benzyl, C 3 -C 6 cycloalkyl and methyl substituted with C 3 -C 6 cycloalkyl; or a pharmaceutically acceptable salt thereof.
- R4 and R5 are each independently selected from H, C 1 -C 6 alkyl, phenyl, benzyl, C 3 -C 6 cycloalkyl and methyl substituted with C 3 -C 6 cycloalkyl; or a pharmaceutically acceptable salt thereof.
- E2 A compound according to embodiment E1, wherein the compound is a compound of formula (Ie),
- R1 and R2 are each independently selected from H, C1-C6 alkyl, benzyl and substituent (i); with the proviso that R1 and R2 cannot both be H;
- R4 and R5 are each independently selected from H, C1-C6 alkyl, phenyl, benzyl, C3-C6 cycloalkyl and methyl substituted with C3-C6 cycloalkyl; or a pharmaceutically acceptable salt thereof.
- R4 and R5 are each independently selected from H, C1-C6 alkyl, phenyl, benzyl, C3-C6 cycloalkyl and methyl substituted with C3-C6 cycloalkyl; or a pharmaceutically acceptable salt thereof.
- E3 The compound or pharmaceutically acceptable salt thereof according to embodiments E1-E2, wherein R1 is substituent (i).
- E13 The compound or pharmaceutically acceptable salt thereof according to embodiment E1, wherein R1 is benzyl; and R2 is selected from H, C1-C6 alkyl, benzyl and substituent (i); and R3 is absent.
- E14 The compound or pharmaceutically acceptable salt thereof according to any of embodiments E1-E13, wherein R4 and R5 are independently selected from H, C1-C6 alkyl, phenyl and benzyl.
- E16 The compound or pharmaceutically acceptable salt thereof according to any of embodiments E1-E15, wherein R4 and R5 are selected from H, C 1 -C 6 alkyl, phenyl and benzyl; and at least one of R4 and R5 is H.
- E17 The compound or pharmaceutically acceptable salt thereof according to any of embodiments E1-E16, wherein R4 and R5 are both H.
- E31 A compound or pharmaceutically acceptable salt thereof according to any of embodiments E1-E29, for use as a medicament.
- E32. The compound or pharmaceutically acceptable salt for use as a medicament according to embodiment E31, wherein said medicament is an oral medicament such as a tablet or a capsule for oral administration.
- a pharmaceutical composition comprising a therapeutically effective amount of the compound or pharmaceutically acceptable salt thereof according to any of embodiments E1- E29, and one or more pharmaceutically acceptable carriers or diluents.
- composition according to any of embodiments E33-E38, wherein said pharmaceutical composition further comprises a compound selected from the group consisting of L-DOPA, a MAO-B inhibitor such as selegiline or rasagiline, a COMT inhibitor such as entacapone or tolcapone, an adenosine 2a antagonist such as istradefylline, an antiglutamatergic agent such as amantadine or memantine, an acetylcholinesterase inhibitor such as rivastigmine, donepezil or galantamine, an antipsychotic agent such as quetiapine, clozapine, risperidone, pimavanserin, olanzapine, haloperidol, aripiprazole or brexpiprazole; or an antibody targeting alpha-synuclein, Tau or A-beta protein.
- a neurodegenerative disease or disorder such as Parkinson's Disease, Huntington’s disease, Restless leg syndrome or Alzheimer’s disease
- a neuropsychiatric disease or disorder such as schizophrenia, attention deficit hyperactivity disorder or drug addiction.
- E41 The compound or pharmaceutically acceptable salt thereof according to any of embodiments E1-E29, for use in the treatment according to embodiment E40, wherein said neurodegenerative disease or disorder is Parkinson's Disease.
- E42 The compound or pharmaceutically acceptable salt thereof according to any of embodiments E1-E29, for use in the treatment according to any of embodiments E40-E41, wherein said compound is to be used in combination with another agent which is useful in the treatment of a neurodegenerative disease or disorder such as Parkinson’s disease.
- E43 The compound or pharmaceutically acceptable salt thereof according to any of embodiments E1-E29, for use in the treatment according to any of embodiments E40-E42, wherein said compound is to be used in combination with a compound selected from the group consisting of L-DOPA, droxidopa, foliglurax, a MAO-B inhibitor such as selegiline or rasagiline, a COMT inhibitor such as entacapone or tolcapone, an adenosine 2a antagonist such as istradefylline, an antiglutamatergic agent such as amantadine or memantine, an acetylcholinesterase inhibitor such as rivastigmine, donepezil or galantamine, an antipsychotic agent such as quetiapine, clozapine, risperidone, pimavanserin, olanzapine, haloperidol, aripiprazole or brexpiprazole; or in combination with an antibody targeting alpha
- E45 The compound or pharmaceutically acceptable salt thereof according to any of embodiments E1-E29, for use in the treatment according to any of embodiments E40-E44, wherein said compound is comprised in an oral pharmaceutical composition such as a tablet or a capsule for oral administration.
- E46. A method for the treatment of a neurodegenerative disease or disorder such as Parkinson's Disease, Huntington’s disease, Restless leg syndrome or Alzheimer’s disease; or a neuropsychiatric disease or disorder such as schizophrenia, attention deficit hyperactivity disorder or drug addiction; which method comprises the administration of a therapeutically effective amount of a compound or pharmaceutically acceptable salt thereof according to any of embodiments E1-E29, to a patient in need thereof.
- E52 Use of a compound or pharmaceutically acceptable salt thereof according to any of embodiments E1-E29, in the manufacture of a medicament for the treatment of a neurodegenerative disease or disorder such as Parkinson's Disease, Huntington’s disease, Restless leg syndrome or Alzheimer’s disease; or for the treatment of a neuropsychiatric disease or disorder such as schizophrenia, attention deficit hyperactivity disorder or drug addiction.
- a neurodegenerative disease or disorder such as Parkinson's Disease, Huntington’s disease, Restless leg syndrome or Alzheimer’s disease
- a neuropsychiatric disease or disorder such as schizophrenia, attention deficit hyperactivity disorder or drug addiction.
- E54 The use according to any of embodiments E52-E53, wherein said medicament is used in combination with another agent which is useful in the treatment of a neurodegenerative disease or disorder such as Parkinson’s disease.
- E55 The use according to any of embodiments E52-E54, wherein said medicament is used in combination with a compound selected from the group consisting of L-DOPA, droxidopa, foliglurax, a MAO-B inhibitor such as selegiline or rasagiline, a COMT inhibitor such as entacapone or tolcapone, an adenosine 2a antagonist such as istradefylline, an antiglutamatergic agent such as amantadine or memantine, an acetylcholinesterase inhibitor such as rivastigmine, donepezil or galantamine, an antipsychotic agent such as quetiapine, clozapine, risperidone, pimavanserin, olanzapine, haloperidol,
- the compounds of formula (Id) may be prepared by methods described below, together with synthetic methods known in the art of organic chemistry, or modifications that are familiar to those of ordinary skill in the art.
- the starting materials used herein are available commercially or may be prepared by routine methods known in the art, such as those methods described in standard reference books such as“Compendium of Organic Synthetic Methods, Vol. I-XII” (published with Wiley-Interscience).
- Preferred methods include, but are not limited to, those described below.
- the schemes are representative of methods useful in synthesizing the compounds of the present invention. They are not intended to constrain the scope of the invention in any way.
- LC-MS methods Analytical LC-MS data were obtained using the methods identified below.
- Method 550 LC-MS were run on Waters Aquity UPLC-MS consisting of Waters Aquity including column manager, binary solvent manager, sample organizer, PDA detector (operating at 254 nM), ELS detector, and TQ-MS equipped with APPI-source operating in positive ion mode.
- LC-conditions The column was Acquity UPLC BEH C18 1.7 ⁇ m; 2.1x50mm operating at 60°C with 1.2 ml/min of a binary gradient consisting of water + 0.05 % trifluoroacetic acid (A) and acetonitrile/water (95:5) + 0.05 % trifluoroacetic acid.
- LC-MS were run on Waters Aquity UPLC-MS consisting of Waters Aquity including column manager, binary solvent manager, sample organizer, PDA detector (operating at 254 nM), ELS detector, and TQ-MS equipped with APPI-source operating in positive ion mode.
- LC-conditions The column was Acquity UPLC HSS T31.8 ⁇ m; 2.1x50mm operating at 60°C with 1.2 ml/min of a binary gradient consisting of water + 0.05 % trifluoroacetic acid (A) and acetonitrile/water (95:5) + 0.05 % trifluoroacetic acid.
- DIPEA Diisopropylethylamine
- MOM-Cl Chloromethyl methyl ether
- Pd/C Palladium on carbon
- TMSCH2N2 Trimethylsilyl diazomethane
- TMSI Trimethylsilyl iodide
- the prodrug with two phosphoric acid moieties on the catechol hydroxyl groups can be prepared from (4aR,10aR)-1-propyl-1,2,3,4,4a,5,10,10a-octahydrobenzo[g]quinoline-6,7-diol hydrochloride by reaction with dibenzyl phosphonate and a suitable base like K 2 CO 3 or DIPEA, but not limited to, followed by global deprotection as described for (4aR,10aR)-1-propyl- 1,2,3,4,4a,5,10,10a-octahydrobenzo[g]quinoline-6,7-diyl bis(phosphate).
- the two mono-benzylated catechol derivatives can be converted to the corresponding mono- phosphates as described for (4aR,10aR)-7-hydroxy-1-propyl-1,2,3,4,4a,5,10,10a- octahydrobenzo[g]quinolin-6-yl phosphate.
- Prodrugs wherein the phosphoric acid is attached via a linker to the N atom can be prepared as described for ((1S,4aR,10aR)-6,7-dihydroxy-1-propyl-1,2,3,4,4a,5,10,10a- octahydrobenzo[g]quinolin-1-ium-1-yl)methyl hydrogen phosphate.
- mixed N-bound phosphate and O-benzyl prodrugs like ((1S,4aR,10aR)-7-(benzyloxy)-6-hydroxy-1-propyl-1,2,3,4,4a,5,10,10a- octahydrobenzo[g]quinolin-1-ium-1-yl)methyl hydrogen phosphate can be prepared.
- 4aR,10aR)-7-(benzyloxy)-6-(methoxymethoxy)-1-propyl-1,2,3,4,4a,5,10,10a- octahydrobenzo[g]quinoline (20 g) in MeOH (140 mL) was added Pd/C (10%, 30 g) under N2. The suspension was degassed under vacuum and purged with H2.
- 4aR,10aR)-6-(methoxymethoxy)-1-propyl-1,2,3,4,4a,5,10,10a- octahydrobenzo[g]quinolin-7-ol 15 g) in MeOH (150 mL) was added drop-wise (trimethylsilyl)diazomethane (2M in ether, 246 mL) at room temperature over 0.5 hours.
- Step 4 Compound (3): (4aR,10aR)-7-methoxy-1-propyl-1,2,3,4,4a,5,10,10a- octahydrobenzo[g]quinolin-6-ol
- the reaction mixture was cooled to 0 °C before MeCN (15 mL), DIPEA (6.66 mL), and dibenzylphosphate (5.02 g) were added.
- the mixture was stirred at 0 °C for 2 hours, before it was partitioned between aqueous KH 2 PO 4 (0.5 M, 50 mL) and EtOAc (20 mL, 30 mL).
- the combined organic layers were washed with brine (20 mL), dried over Na 2 SO 4 , filtered, and concentrated.
- the reaction mixture was cooled to 0 °C before CCl 4 (6 mL), DIPEA (9.91 mL), and dibenzylphosphate (7.46 g) were added.
- the mixture was stirred at 0 °C for 2 hours, before it was partitioned between aqueous KH 2 PO 4 (0.5 M, 50 mL) and EtOAc (20 mL and 30 mL).
- the combined organic phases were washed with brine (20 mL), dried over Na 2 SO 4 , filtered, and concentrated.
- the residue was purified twice by prep-HPLC using a Shimadzhu LC20AP instrument (run 1: Phenomenex Luna C18 250*50 mm, 10 ⁇ m particles column operated at room temperature with 80 mL/min of a gradient of water + 0.1 % TFA (A) and MeCN (B): 0-20 minutes 25% B to 55% B; 20.1-25 minutes 100% B; 25.1-30 minutes 25% B.
- Shimadzhu LC20AP instrument run 1: Phenomenex Luna C18 250*50 mm, 10 ⁇ m particles column operated at room temperature with 80 mL/min of a gradient of water + 0.1 % TFA (A) and MeCN (B): 0-20 minutes 25% B to 55% B; 20.1-25 minutes 100% B; 25.1-30 minutes 25% B.
- Run 2 Phenomenex Luna C18250*40 mm, 10 ⁇ m particles column operated at room temperature with 60 mL/min of a gradient of water + 0.1 % TFA (A) and MeCN (B): 0-10 minutes 35% B to 55% B; 10.1-12 minutes 100% B; 12.1-15 minutes 35% B) to afford the title compound (0.2 g).
- the flask was sealed with a septum and evacuated and backfilled with argon (this procedure was repeated 3 times).
- Degassed methanol 80 mL was added, followed by addition of benzyl bromide (1.60 mL) and NaOH (1.07 g).
- the mixture was stirred at room temperature for 10 minutes under argon atmosphere, then heated to 60 °C and stirred for additional 90 minutes.
- the mixture was cooled to room temperature and concentrated under reduced pressure, then diluted with aqueous sodium bicarbonate (100 mL) and EtOAc (100 mL).
- Step 2 Benzyl (((1S,4aR,10aR)-6,7-bis(benzyloxy)-1-propyl-1,2,3,4,4a,5,10,10a- octahydrobenzo[g]quinolin-1-ium-1-yl)methyl) phosphate (4aR,10aR)-6,7-bis(benzyloxy)-1-propyl-1,2,3,4,4a,5,10,10a-octahydrobenzo[g]quinoline (200 mg), dibenzyl chloromethyl phosphate (296 mg), NaI (272 mg, 1.812 mmol) and cesium carbonate (443 mg, 1.36 mmol) were dissolved in anhydrous acetonitrile (5.0 mL) and the resulting solution is stirred at 40 °C for 90 minutes under argon atmosphere.
- Step 3 ((1S,4aR,10aR)-6,7-dihydroxy-1-propyl-1,2,3,4,4a,5,10,10a- octahydrobenzo[g]quinolin-1-ium-1-yl)methyl hydrogen phosphate
- the pH value of the supernatant was then measured and adjusted to 7.4 ⁇ 0.1 by adding 1% phosphoric acid or 1 N sodium hydroxide.2 mL of dosing solution (50 mM for test compounds and 100 mM for positive control (propantheline bromide)) was mixed with 98 ⁇ L of blank plasma to achieve 1 mM test compund and 2 mM positive control of final concentration. The mixture was incubated, and samples were withdrawn from the incubations at the pre-determined time points of 0, 0.5, 1, 2, 4 and 6 hours (in duplicate) at 37 °C in water bath.
- Example 1b Conversion of compounds of the invention in human hepatocytes Incubations were conducted in 96-well plates at 1 ⁇ M compound concentration in duplicate. The hepatocyte cell concentration was 0.5 ⁇ 106 cells/mL used for final incubation at 37 °C in an incubator of 5% CO295% relative humidity. The medium control samples were included at 0 and 60 minutes in the absence of cells. The total organic concentration was £ 1% (DMSO £ 0.1%) in the final incubation.
- the controls (7-ethoxycoumarin and 7-hydroxycoumarin) was incubated parallel at 3 ⁇ M.2 mL of dosing solution (50 mM for test compounds and 100 mM for positive control) was mixed with 98 ⁇ L of 100 mM PBS to achieve 1 mM test compund and 2 mM positive control of final concentration. The mixture was incubated, and samples were withdrawn from the incubations at pre-determined time points of 0, 0.5, 1, 2, 4 and 6 hours (in duplicate) at 37 °C in water bath.
- Example 2 5-HT2B agonist activity and binding assay 5-HT2B agonist activity assay Evaluation of the agonist activity of compounds (I), (Ia), (Ib), (Ic), compound (2), compound (3), compound (6), compound (8), and compound (9) at the human 5-HT2B receptor was performed by Eurofins/Cerep (France) measuring the compound effects on inositol monophosphate (IP1) production using the HTRF detection method. Briefly, the human 5- HT2B receptor was expressed in transfected CHO cells.
- the cells were suspended in a buffer containing 10 mM Hepes/NaOH (pH 7.4), 4.2 mM KCl, 146 mM NaCl, 1 mM CaCl2, 0.5 mM MgCl 2 , 5.5 mM glucose and 50 mM LiCl, then distributed in microplates at a density of 4100 cells/well and incubated for 30 minutes at 37 °C in the presence of buffer (basal control), test compound or reference agonist.
- buffer basic control
- test compound or reference agonist for stimulated control measurement, separate assay wells contained 1 ⁇ M 5-HT.
- the cells were lysed and the fluorescence acceptor (fluorophen D2-labeled IP1) and fluorescence donor (anti-IP1 antibody labeled with europium cryptate) were added. After 60 minutes at room temperature, the fluorescence transfer was measured at lambda(Ex) 337 nm and lambda(Em) 620 and 665 nm using a microplate reader (Rubystar, BMG). The IP1 concentration was determined by dividing the signal measured at 665 nm by that measured at 620 nm (ratio). The results were expressed as a percent of the control response to 1 ⁇ M 5-HT.
- fluorescence acceptor fluorophen D2-labeled IP1
- fluorescence donor anti-IP1 antibody labeled with europium cryptate
- the standard reference agonist was 5-HT, which was tested in each experiment at several concentrations to generate a concentration- response curve from which its EC 50 value is calculated as described above for dopamine functional assays.
- 5-HT2B binding assay Evaluation of the affinity of compounds for the human 5-HT2B receptor was determined in a radioligand binding assay at Eurofins/Cerep (France).
- Membrane homogenates prepared from CHO cells expressing the human 5HT2B receptor were incubated for 60 minutes at room temperature with 0.2 nM [125I]( ⁇ )DOI (1-(4-iodo-2, 5-dimethoxyphenyl)propan-2-amine) in the absence or presence of the test compound in a buffer containing 50 mM Tris-HCl (pH 7.4), 5 mM MgCl2, 10 ⁇ M pargyline and 0.1% ascorbic acid. Nonspecific binding is determined in the presence of 1 ⁇ M ( ⁇ )DOI.
- Example 3 PK experiments in rats For all the experiments, blood samples of approximately 0.68 mL were drawn from the tail or sublingual vein and put into K3EDTA tubes that had been pre-cooled and prepared with stabilizing solution consisting of 80 ⁇ L ascorbic acid and 40 ⁇ L 100 mM D-saccharic acid 1,4 lactone in water. The tubes were inverted gently 6-8 times to ensure thorough mixing and then placed in wet ice. The collecting tube was placed in wet ice for up to 30 minutes until centrifugation. Once removed from the wet ice the centrifugation was initiated immediately. Immediately after end of centrifugation the samples were returned to wet ice.
- concentration-time data was analyzed, using standard software using appropriate noncompartmental techniques to obtain estimates of the derived PK parameters.
- Mobile phase A 20 mM ammonium formate (aq) + 0.5% formic acid.
- Mobile phase B Acetonitrile.
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AR113908A1 (es) | 2017-11-24 | 2020-06-24 | H Lundbeck As | Profármacos de catecolamina para uso en el tratamiento de la enfermedad de parkinson |
US11168056B2 (en) | 2019-05-20 | 2021-11-09 | H. Lundbeck A/S | Process for the manufacturing of (6aR,10aR)-7-propyl-6,6a,7,8,9,10,10a,11-octahydro-[1,3]dioxolo[4′,5′:5,6]benzo[1,2-G]quinoline and (4aR,10aR)-1-propyl-1,2,3,4,4a,5,10,10a-octahydro-benzo[G]quinoline-6,7-diol |
US11104697B2 (en) | 2019-05-20 | 2021-08-31 | H. Lundbeck A/S | Process for the manufacture of (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(((4AR,10AR)-7-hydroxy-1- propyl-1,2,3,4,4A,5,10,10A-octahydrobenzo[g]quinolin-6-yl)oxy)tetrahydro-2H-pyran-2-carboxylic acid |
US11130775B2 (en) | 2019-05-20 | 2021-09-28 | H. Lundbeck A/S | Solid forms of (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(((4aR,10aR)-7-hydroxy-1-propyl-1,2,3,4,4A,5,10,10A-octahydrobenzo[g]quinolin-6-yl)oxy)tetrahydro-2H-pyran-2-carboxylic acid |
US11111263B2 (en) | 2019-05-20 | 2021-09-07 | H. Lundbeck A/S | Process for the manufacture of (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(((4aR,10aR)-7-hydroxy-1-propyl-1,2,3,4,4a,5,10,10a-octahydrobenzo[g]quinolin-6-yl)oxy)tetrahydro-2H-pyran-2-carboxylic acid |
US20240025857A1 (en) | 2020-11-17 | 2024-01-25 | H. Lundbeck A/S | New catecholamine prodrugs for use in the treatment of parkinson's disease |
WO2023208865A1 (en) | 2022-04-25 | 2023-11-02 | Integrative Research Laboratories Sweden Ab | NOVEL 1,2,3,4,4a,5,6,7,8,9,10,10a-DODECAHYDROBENZO[G]QUINOLIN-6-OL COMPOUNDS AND USES THEREOF |
WO2023208869A1 (en) | 2022-04-25 | 2023-11-02 | Integrative Research Laboratories Sweden Ab | NOVEL ESTERS OF 1,2,3,4,4a,5,6,7,8,9,10,10a-DODECAHYDROBENZO[G]QUINOLIN-6-OL COMPOUNDS AND USES THEREOF |
WO2023208867A1 (en) | 2022-04-25 | 2023-11-02 | Integrative Research Laboratories Sweden Ab | NOVEL 1,2,3,4,4a,5,8,9,10,10a-DECAHYDROBENZO[G]QUINOLIN-6(7H)-ONE COMPOUNDS AND USES THEREOF |
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US3132171A (en) | 1962-06-18 | 1964-05-05 | Strong Cobb Arner Inc | 3, 4-diphosphatophenyl-alanine and process for making same |
US4543256A (en) | 1982-03-17 | 1985-09-24 | Northeastern University | (-)-10,1L Methylenedioxy-N-N-propylnoraporphine and methods employing it for inhibiting the effects of epileptic seizures and for prevention and treatment of duodenal ulcers |
IT1213182B (it) | 1984-06-25 | 1989-12-14 | Simes | Derivati di composti a struttura catecolamminica. |
EP0393781B1 (de) | 1989-04-20 | 1995-02-08 | ZAMBON GROUP S.p.A. | Dopamin-Medikament-Vorstufe |
SE0001438D0 (sv) | 2000-04-18 | 2000-04-18 | Axon Chemicals Bv | New chemical compounds and their use in therapy |
SE0102036D0 (sv) | 2001-06-08 | 2001-06-08 | Axon Biochemicals Bv | Pharmaceutical formulation for the efficient administration of apomorphine, 6aR- (-) -N- Propyl- norapomorphine and their derivatives and pro-drugs thereof |
US7101912B2 (en) | 2002-12-06 | 2006-09-05 | Xenoport, Inc. | Carbidopa prodrugs and derivatives, and compositions and uses thereof |
TWI404702B (zh) | 2007-08-31 | 2013-08-11 | Lundbeck & Co As H | 兒茶酚胺衍生物和其前藥 |
TW201036949A (en) * | 2009-02-27 | 2010-10-16 | Lundbeck & Co As H | Treatment of dyskinesia related disorders |
TW201035054A (en) * | 2009-02-27 | 2010-10-01 | Lundbeck & Co As H | Methods of administering (4aR, 10aR)-1-n-propyl-1,2,3,4,4a,5,10,10a-octahydro-benzo[g]quinoline-6,7-diol and pharmaceutical compositions thereof |
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AR113908A1 (es) * | 2017-11-24 | 2020-06-24 | H Lundbeck As | Profármacos de catecolamina para uso en el tratamiento de la enfermedad de parkinson |
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